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首页> 外文期刊>Molecular Biotechnology >Cloning, Characterization, and Expression of a New cry1Ab Gene from DOR Bt-1, an Indigenous Isolate of Bacillus thuringiensis
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Cloning, Characterization, and Expression of a New cry1Ab Gene from DOR Bt-1, an Indigenous Isolate of Bacillus thuringiensis

机译:苏云金芽孢杆菌本土分离物DOR Bt-1的cry1Ab新基因的克隆,鉴定和表达

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A new cry1Ab gene was cloned from the promising local isolate, DOR Bt-1, a Bacillus thuringiensis strain isolated from castor semilooper (Achaea janata L.) cadavers from castor bean (Ricinus communis L.) field. The nucleotide sequence of the cloned cry1Ab gene indicated that the open reading frame consisted of 3,465 bases encoding a protein of 1,155 amino acid residues with an estimated molecular weight of 130 kDa. Homology comparisons revealed that the deduced amino acid sequence of cry1Ab had a variation of seven amino acid residues compared to those of the known Cry1Ab proteins in the NCBI database and this gene has been designated as cry1Ab26 by the B. thuringiensis δ-endotoxin Nomenclature Committee. cry1Ab26 was cloned into pET 29a(+) vector and expressed in E. coli strain BL21 (DE3) under the control of T7 promoter with IPTG induction. ELISA, SDS-PAGE, and Western blot analysis confirmed the expression of 130-kDa protein. Insect bioassays with neonate larvae of Helicoverpa armigera showed that the partially purified Cry1Ab26 caused 97 % mortality within 5 days of feeding.
机译:从有前途的本地分离株DOR Bt-1(一种从蓖麻(Ricinus communis L.)田地的蓖麻半loop(Achaea janata L.)尸体中分离到的苏云金芽孢杆菌菌株)中克隆了一个新的cry1Ab基因。克隆的cry1Ab基因的核苷酸序列表明,开放阅读框由3,465个碱基组成,编码1,155个氨基酸残基的蛋白质,估计分子量为130 kDa。同源性比较显示,与NCBI数据库中已知的Cry1Ab蛋白相比,cry1Ab推导的氨基酸序列具有七个氨基酸残基的变异,该基因已被苏云金芽孢杆菌δ-内毒素命名委员会命名为cry1Ab26。将cry1Ab26克隆到pET 29a(+)载体中,并在IPTG诱导的T7启动子控制下在大肠杆菌BL21(DE3)中表达。 ELISA,SDS-PAGE和Western blot分析证实了130 kDa蛋白的表达。用棉铃虫新生幼虫进行的昆虫生物测定表明,部分纯化的Cry1Ab26在喂食后5天内导致97%的死亡率。

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